Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3031984

FEI Number

3001237472

Entity Name

SPECIALTY SURGICAL PRODUCTS, INC.

City/State/Country

VICTOR, MT, US

Establishment Address

1123 NORTH U.S. HWY. 93, VICTOR, MT 59875, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

SPECIALTY SURGICAL PRODUCTS, INC. (Owner Number: 9031344)

Owner / Operator Contact Address

1123 NORTH U.S. HWY. 93, --, Victor, MT 59875, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K973082

PMA Number

N/A

All Registered Proprietary Names

PEDIATRIC ANAL DILATOR Clear Cast Silicone Silo Bag

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FFP	Dilator, Rectal	Gastroenterology, Urology	Class 1	876.5450	1998-10-01
FTL	Mesh, Surgical, Polymeric	General, Plastic Surgery	Class 2	878.3300	2008-02-11

Official Correspondent

Angela Lawrence

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

SPECIALTY SURGICAL PRODUCTS, INC.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K220540	Covidien	ProGrip Self-Gripping Polypropylene Mesh	2022-09-22

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3031984. Last updated year: 2026. Please use registration number 3031984 when referencing this establishment in official correspondence.